| Literature DB >> 36115892 |
Lulin Huang1,2, Runze Li1, Lin Ye1, Shanshan Zhang1, Huaping Tian1, Mingyan Du1, Chao Qu3, Shujin Li1, Jie Li3, Mu Yang1, Biao Wu4, Ran Chen4, Guo Huang1, Ling Zhong1, Hongjie Yang5, Man Yu3, Yi Shi1, Changguan Wang6, Houbin Zhang1, Wei Chen4, Zhenglin Yang7,8.
Abstract
The human retina serves as a light detector and signals transmission tissue. Advanced insights into retinal disease mechanisms and therapeutic strategies require a deep understanding of healthy retina molecular events. Here, we sequenced the mRNA of over 0.6 million single cells from human retinas across six regions at nine different ages. Sixty cell sub-types have been identified from the human mature retinas with unique markers. We revealed regional and age differences of gene expression profiles within the human retina. Cell-cell interaction analysis indicated a rich synaptic connection within the retinal cells. Gene expression regulon analysis revealed the specific expression of transcription factors and their regulated genes in human retina cell types. Some of the gene's expression, such as DKK3, are elevated in aged retinas. A further functional investigation suggested that over expression of DKK3 could impact mitochondrial stability. Overall, decoding the molecular dynamic architecture of the human retina improves our understanding of the vision system.Entities:
Keywords: aging; deep Sc-RNA sequencing; human retina
Year: 2022 PMID: 36115892 DOI: 10.1007/s11427-021-2163-1
Source DB: PubMed Journal: Sci China Life Sci ISSN: 1674-7305 Impact factor: 10.372